Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey-Reference-Cited by-同舟云学术

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Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey

Published:2003-01-21 Issue:3 Volume:162 Page:154-158
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Tekin M.,Duman T.,Boğoçlu G.,İncesulu A.,Çomak E.,Fitoz S.,Yılmaz E.,İlhan İ.,Akar N.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00431-002-1129-z.pdf

Reference27 articles.

1. Abe S, Usami S, Shinkawa H, Kelley PM, Kimberling WJ (2000) Prevalent connexin 26 gene (GJB2) mutations in Japanese. J Med Genet 37: 41–43

2. Abe S, Kelley PM, Kimberling WJ, Usami S (2001) Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-G mitochondrial mutation. Am J Med Genet 103: 334–338

3. Akar N (1998) Site specific mutagenesis: usage for the mutation detection in thrombosis. Turk J Haematol 15: 123–124

4. Akar N, Akar E, Yilmaz E (2000) Coexistence of Factor V 1691 G-A and Factor V 4070 A-G mutation in Turkish thromboembolic patients. Am J Hematol 65: 88

5. Casano RA, Johnson DF, Bykovskaya Y, Toricelli F, Bigozzi M, Fischel-Ghodsian N (1999) Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications. Am J Otolaryngol 20: 151–156

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2. Crucial Roles of the m.1555A>G Mutation on MT-RNR1 Gene in Hearing Loss;J BIOL REG HOMEOS AG;2022

3. Mitochondrial 12s rRNA mutation A1555G: validation of a genotyping method;Minerva Biotechnology and Biomolecular Research;2022-05

4. Novel m.4268T>C mutation in the mitochondrial tRNAIle gene is associated with hearing loss in two Chinese families;World Journal of Clinical Cases;2022-01-07

5. Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China;International Journal of Pediatric Otorhinolaryngology;2018-05

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